3-Methoxypropylamine → N-(3-Methoxypropyl)-6-[[1-(4-methylphenyl)-2-propylmercapto-1H-benzimidazol-6-yl]oxy]Hexanamide
Reaction equation
C[O:2][C:3](=O)[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][O:9][C:10]1[CH:11]=[CH:12][C:13]2[N:17]=[C:16]([S:18][CH2:19][CH2:20][CH3:21])[N:15]([C:22]3[CH:27]=[CH:26][C:25]([CH3:28])=[CH:24][CH:23]=3)[C:14]=2[CH:29]=1.[CH3:31][O:32][CH2:33][CH2:34][CH2:35][NH2:36]>>[CH3:31][O:32][CH2:33][CH2:34][CH2:35][NH:36][C:3](=[O:2])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][O:9][C:10]1[CH:11]=[CH:12][C:13]2[N:17]=[C:16]([S:18][CH2:19][CH2:20][CH3:21])[N:15]([C:22]3[CH:27]=[CH:26][C:25]([CH3:28])=[CH:24][CH:23]=3)[C:14]=2[CH:29]=1Participants
3
Procedure
100 mg of 6-[[1-(4-methylphenyl)-2-propylmercapto-1H-benzimidazol-6-yl]oxy]hexanoic acid methyl ester was reacted with 3-methoxypropylamine according to general operating instructions 4. 38 mg was obtained.
Workup
- custom38 mg was obtained
Sources & evidence
- ORD record
- ord-15f784488f5b4d3ba770b147ab5ee25f
- Source dataset
- uspto-grants-2007_03
- Patent number
- US07196202B2
Reaction notes
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